Department of Veterinary Microbiology, School of Veterinary Medicine, Azabu University, 1-17-71 Fuchinobe, Sagamihara, Kanagawa 252-5201, Japan.
J Clin Immunol. 2013 Jul;33(5):977-83. doi: 10.1007/s10875-013-9880-7. Epub 2013 Mar 16.
Japanese cedar (Cryptomeria japonica; CJ) pollinosis is a type I allergy induced by CJ pollen, and Cry j 2 is one of the major allergens in this pollen. In a previous study, we analyzed IgE epitopes on Cry j 2 in humans by using synthetic peptides. The main purpose of this study was to identify B-cell epitopes on Cry j 2 in patients with CJ pollinosis by using monoclonal antibodies (mAbs) for Cry j 2.
We used ELISA with mAbs for the epitope analysis. Sera samples were collected from 80 patients with CJ pollinosis, and allergenic epitopes for mAbs and human IgE were identified using ELISA with synthetic peptides. The importance of the epitopes for human IgE was analyzed using an inhibition ELISA.
Four independent epitopes (epitope #1, #2, #3, and #4) were identified on Cry j 2 with the use of mAbs. Epitope #3 and #4, corresponding to peptides No. 25 and No. 33, respectively, were newly determined as epitopes for mAbs and human IgE. Inhibition ELISA showed that not only epitope #2 (sequential) but epitope #1 (conformational) may play an important role in the CJ pollinosis.
Our results revealed 4 epitopes, including two new ones, on Cry j 2. We also found that inhibition ELISA with appropriate mAbs could be a viable method of evaluating the importance of the conformational and sequential epitopes for human IgE. These results are beneficial for the development of safer and more efficient therapeutic strategies for treating CJ pollinosis.
日本扁柏(Cryptomeria japonica;CJ)花粉症是由 CJ 花粉引起的 I 型过敏,Cry j 2 是该花粉中的主要过敏原之一。在之前的研究中,我们使用合成肽分析了人类 Cry j 2 上的 IgE 表位。本研究的主要目的是使用 Cry j 2 的单克隆抗体(mAbs)鉴定 CJ 花粉症患者 Cry j 2 上的 B 细胞表位。
我们使用 ELISA 结合 mAbs 进行表位分析。从 80 名 CJ 花粉症患者中采集血清样本,使用 ELISA 结合合成肽鉴定 mAbs 和人 IgE 的过敏原表位。使用抑制 ELISA 分析表位对人 IgE 的重要性。
使用 mAbs 鉴定出 Cry j 2 上的 4 个独立表位(表位#1、#2、#3 和#4)。表位#3 和#4,分别对应于肽 No.25 和 No.33,被确定为 mAbs 和人 IgE 的新表位。抑制 ELISA 显示,不仅表位#2(序列),而且表位#1(构象)可能在 CJ 花粉症中发挥重要作用。
我们的研究结果揭示了 Cry j 2 上的 4 个表位,包括 2 个新表位。我们还发现,使用适当的 mAbs 进行抑制 ELISA 可能是评估构象和序列表位对人 IgE 重要性的可行方法。这些结果有助于开发更安全、更有效的治疗 CJ 花粉症的治疗策略。